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RecruitingNCT06614179Updated Sep 26, 2024

A Pan-cancer Screening and Diagnosis Model Based on Abdominal CT Was Established

An observational study in Abdominal Neoplasm, sponsored by Xiangdong Cheng. Recruiting at 2 sites in China. Open to participants aged 18 Years to 75 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-09-26.

Sponsored by Xiangdong Cheng · Observational

From the registry’s dates

  • Started Jul 2024; still recruiting 2 years 3 months later.
Study type
Observational
Model
Case-only
Time perspective
Retrospective
Enrollment
100,000
Ages
18 Years to 75 Years
Sex
All
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Study summary

Abdominal noncontrast scan and contrast-enhanced CT were used to establish a screening and diagnostic model for abdominal tumors

Read the detailed description

Secondary objective: To establish a grading model of abdominal tumors based on clinical indicators Exploratory Objective: To include CT scans in large-scale non-tumor populations for validation and to improve model accuracy Certainty

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Conditions studied

  • Abdominal Neoplasm

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03

In context

Abdominal Neoplasms

67 studies on the registry are indexed under Abdominal Neoplasms; 18 are open to participants now.

This study's planned enrollment of 100,000 is above the median of 100 across 15 observational studies indexed under Abdominal Neoplasms.

Browse Abdominal Neoplasms studies →

Lead sponsor

Xiangdong Cheng is the lead sponsor of 6 studies on the registry; 6 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Patients with abdominal tumors or Non-tumor population

Inclusion criteria

  • Patients with abdominal tumors:
  • all patients were pathologically diagnosed with abdominal tumors;
  • The clinical case data of all patients were complete, and complete follow-up was obtained, with clear information on medical visits, operation time and survival status within 2 years. If the cause of death is unknown, it will be recorded as censored data;
  • All patients had no history of active abdominal bleeding, no serious infection or other abdominal diseases that affected the observation of CT imaging within 3 months before surgery.
  • Non-tumor population:
  • all patients have complete clinical case data, complete abdominal CT, no history of malignant tumors, no serious infections or other abdominal diseases that affect the diagnosis and observation of CT imaging.

Exclusion criteria

Exclusion Criteria:

  • Cases in which contrast-enhanced or noncontrast CT images show unclear lesions, with significant noise and artifacts;
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Study design

Observational model
Case-only
Time perspective
Retrospective
Enrollment
100,000 participants (estimated)
Patient registry
No
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What researchers measure

Primary outcomes

  1. Whether or not there is a diagnosis of abdominal tumor questionnaire

    Whether or not there is a diagnosis of abdominal tumor

    Time frame: first visited at baseline

07

Study locations

2 of 2 sites recruiting
  • Cancer Hospital of the University of Chinese Academy of Sciences (Zhejiang Cancer Hospital)
    Hangzhou, Zhejiang 310000, China
    Recruiting
  • Zhejiang Cancer Hospital;Cancer hospital of the university of chinese academy of sciences
    Hangzhou, Zhejiang 310022, China
    • Pengfei Yu, MD,PhD · Contact · ypfzmu@163.com · +86-571-88128031
    • Xiangdong Cheng, MD,PhD · Principal investigator
    • Yu Pengfei, MD,PhD · Sub investigator
    Recruiting
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References and documents

Individual participant data

Plan to share: Yes — Abdominal noncontrast scan and contrast-enhanced CT were used to establish a screening and diagnostic model for abdominal tumors

Supporting information: Study protocol

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 26, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06614179
Lead sponsor
Xiangdong Cheng
Responsible party
Xiangdong Cheng (Professor, Zhejiang Cancer Hospital) — Sponsor-investigator
First posted
Sep 26, 2024
Start date
Jul 1, 2024
Primary completion
Dec 31, 2029 (estimated)
Completion
Dec 31, 2029 (estimated)
Last update
Sep 26, 2024

Study contacts

Xiangdong Cheng
Contact
Chengxd516@126.com
0086-571-881280
Can Hu
Contact
chengxd@zjcc.org.cn
13968032995
Xiangdong Cheng
principal investigator · Zhejiang Cancer Hospital

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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